Powerled TM

PWD30 Dual Navy Ship Retrofit KIT

Registry build 21.09.26
6manufacturers in China registered for this device type
1catalogue number
6recalls on this code

Who Else Makes It

Concentrated in Guangdong (2), Shanghai (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code FTD
Manufacturer City Province Registered as Device types
Shanghai Huifeng Medical Instrument Co., Ltd. Shanghai Shanghai Contract manufacturer 4
Dragon Medical Co., Ltd. Suzhou Jiangsu Contract manufacturer 48
Shenzhen Comen Medical Instruments Co., Ltd. Shenzhen Guangdong Contract manufacturer 24
HI-Life Technology (Hebei) Co., Ltd. Bazhou Hebei Manufacturer 11
Shenzhen Youmay Electronics Co., Ltd. Shenzhen Guangdong Manufacturer 10
Shanghai PAX Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 7

Record

Regulatory record for Powerled TM
Listed by Maquet Gmbh, Germany
FDA product code FTD
Device type Lamp, Surgical
Device class Class 2
Regulation 21 CFR 878.4580
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K070442
Record published 2020-09-14
Record revised 2022-12-12 (version 4)

Specifications

Specifications
MRI safety MR Unsafe
Label carries manufacturing date, serial number
Storage Handling environment temperature -10 to 60 °C; Storage environment temperature -10 to 60 °C; Handling environment humidity 20 to 75 % RH; Storage environment humidity 20 to 75 % RH; Handling environment atmospheric pressure 50 to 106 KiloPascal; Storage environment atmospheric pressure 50 to 106 KiloPascal

Catalogue Numbers

Catalogue numbers for Powerled TM
Catalogue number Size Status
ARD267800340A In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Maquet PowerLED II Maquet Gmbh 1,930
S300 Series Dentis Co., Ltd. 41
Standop Volista® Maquet Gmbh 32
L400 Series Dentis Co., Ltd. 24
M400 Series (Ceiling, Mobile) Dentis Co., Ltd. 24
Lamp, Surgical Maquet Gmbh 18
Maquet Ezea Maquet Gmbh 18
Maisilide Shandong Deman Medical Equipment Group Co., Ltd. 15
S250 Series(Ceiling, Mobile) Dentis Co., Ltd. 11
Lucea LED® Maquet Gmbh 7
StarTrol Huot Instruments, LLC 7
Rolite Volista Standop Maquet Gmbh 5

Showing 12 of 52. All products under Lamp, Surgical

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2009-10-07 Not classified Device Design Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturers. All incidents pertain to a crack on the front joint of the Acrobat arm. 39 2012-06-04
2009-10-07 Not classified Device Design Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturers. All incidents pertain to a crack on the front joint of the Acrobat arm. 3 2012-06-04
2009-10-07 Not classified Device Design Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturers. All incidents pertain to a crack on the front joint of the Acrobat arm. 1 2012-06-04
2009-10-07 Not classified Device Design Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturers. All incidents pertain to a crack on the front joint of the Acrobat arm. 166 2012-06-04
2009-02-23 Not classified Device Design The screws holding the Prismatic triple surgical lights may break due to dynamic multidirectional bending stress. The firm has received one complaint report. 54 of all units, both article numbers 2009-09-29
2009-02-23 Not classified Device Design The screws holding the Prismatic triple surgical lights may break due to dynamic multidirectional bending stress. The firm has received one complaint report. 54 of all units, both article numbers 2009-09-29

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer